Validation - Wireless Dataloggers

Validation - Wireless Dataloggers

Precise temperature, pressure and humidity data loggers, designed to deliver accurate, reliable and traceable data collected during your verification, validation and mapping exercises.  Rated to 10Bar and  -80 °C to 150 °C (400 °C with thermal barrier) allows you to use our equipment in anything from a ULT freezer to an autoclaves and depyrogenation oven.

Ethylene Oxide sterilisersEthylene Oxide sterilisers

Validation engineers in charge of EtO sterilisation are required to precisely collect and verify temperature and humidity data from within chambers being purged with Ethylene Oxide.  Our solutions deliver accurate data via single and multi channel offerings in real-time to your computer, with ATEX and/or IS certification.

Chamber ValidationChamber Validation

Validate stability chambers and incubators in compliance with ICH guidelines using precise, calibrated temperature and humidity data loggers, supported with sophisticated, user friendly software compliant to FDA 21 CFR Part 11 for data security and traceability.  GxP and software validation documentation assists you in the process of validating and deploying the system.

Steriliser, Autoclave and Retort ValidationSteriliser, Autoclave and Retort Validation

Wireless data loggers reduce the time taken to configure, perform and analyse temperature, humidity and pressure data collected from inside, high temperature and pressure environments, making them ideal for validating, autoclaves, sterilisers, retorts, lyophilisation and depyrogenation processes. Our solutions offer improved accuracy, repeatability and response times against traditional systems using exposed junction thermocouples.  Equally important is product confidence, we are proud that our solutions are proven to operate and continue to operate for over 10 years. Supported with Calibration certification and sophisticated, user friendly software compliant to FDA 21 CFR Part 11 for data security and traceability. GxP and software validation documentation assist you in validating the system.

IV SterilisationIV Sterilisation

Validation of intravenous delivery systems (IV bags) requires the deployment of a miniature data logger measuring precise temperature data from within with the IV bag via an accurate and responsive external probe, a waterproof connector is used to ensure there is no leakage and radio technology to transmit real-time data. Supported with 21 CFR Part 11 software and GxP validation documents.




Can't find what you are after? or call us on +44 (0)1202 723000


 
© Copyright 2008-2012 Wessex Power Technology Ltd.  | Site Map| Privacy Policy| Register| Client Login| Contact Us
A Yammayap of